Evidence map›Paper›PMID 40411493›Full record

ArticleEpilepsia2025

Serial correlation between saliva and blood beta-hydroxybutyrate levels in children commencing the ketogenic diet for epilepsy.

Neha Kaul, Jing Duan, Dong Cui, Michael Erlichster, Zhibin Chen, Dovile Anderson, Jianxiong Chan, Ingrid E Scheffer, Efstratios Skafidas, Jianxiang Liao and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in Epilepsia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07495267 (Nutritional Ketosis as a Novel Therapeutic Strategy to Stabilize Chronic Aortic Dissection in Marfan Syndrome), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07495267 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

Nutritional Ketosis as a Novel Therapeutic Strategy to Stabilize Chronic Aortic Dissection in Marfan Syndrome

TypeinterventionalSponsorWashington University School of MedicineRan2026 to 2028Enrolled15ConditionsMarfan Syndrome, Aortic DissectionArmsKetogenic diet
3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Neha KaulDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0003-0790-5200
Jing DuanDepartment of Neurology, Shenzhen Children's Hospital, Shenzhen, China.
Dong CuiDepartment of Neurology, Shenzhen Children's Hospital, Shenzhen, China.
Michael ErlichsterMX3 Pty Ltd, Parkville, Victoria, Australia.
Zhibin ChenDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-1888-6917
Dovile AndersonMonash Proteomics, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0003-0284-471X
Jianxiong ChanDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0002-0352-6935
Ingrid E SchefferDepartment of Medicine, Austin Health, University of Melbourne, Heidelberg, Victoria, Australia.ORCID https://orcid.org/0000-0002-2311-2174
Efstratios SkafidasMX3 Pty Ltd, Parkville, Victoria, Australia.ORCID https://orcid.org/0000-0003-4263-9972
Jianxiang LiaoDepartment of Neurology, Shenzhen Children's Hospital, Shenzhen, China.
Patrick KwanDepartment of Neuroscience, School of Translational Medicine, Monash University, Melbourne, Victoria, Australia.ORCID https://orcid.org/0000-0001-7310-276X

Funding

High-level Hospital Construction Project of Guangdong Provincial People's Hospital SZXK033National Health & Medical Research Council GNT2025849Sanming Project of Medicine in Shenzen Municipality SZSM202311028Shenzhen Fund for Guangdong Provincial High-level Clinical Key Specialties SZGSP012
6 · The paper itself

Abstract

objectivesAccurate and user-friendly methods to measure beta-hydroxybutyrate (BHB) concentration are needed to guide the optimal use of ketogenic diet therapy (KDT). We aimed to determine the correlation between serum, capillary, and salivary BHB concentration, and to validate an electrochemical salivary BHB point-of-care test (POCT) in children commencing KDT for drug-resistant epilepsy.

methodsThis was a single center, prospective cohort study. Children <18 years with drug-resistant epilepsy electively admitted to Shenzhen Children's Hospital to initiate KDT between January 1, 2020 and June 30, 2021, were included. Over the 7-day admission, we collected paired saliva and capillary blood samples twice a day and serum blood samples on the first and last days of admission from each participant. Salivary BHB was measured using liquid chromatography mass spectrometry (LCMS) and the POCT. Primary outcome was the correlation between serum and salivary BHB concentration measured using LCMS. Secondary outcomes were the correlation between both the capillary blood and salivary BHB concentration, measured by LCMS, and the POCT device.

resultsSeventy-one serum and 334 capillary blood paired with salivary samples were collected from 42 children (median age 4.5 years, interquartile range 1 to 8 years, 45% female). Salivary BHB measured using LCMS strongly correlated with serum BHB (Spearman's ρ = 0.910) and capillary blood BHB concentrations (Spearman's ρ = 0.865). Salivary BHB concentration was 6% and 7% of serum and capillary blood BHB concentration, respectively. The POCT demonstrated excellent test-retest reliability when compared with LCMS (ICC(A,k) = 0.983, 95% confidence interval: 0.980-0.986). Salivary BHB concentration measured by the POCT showed good accuracy in predicting the capillary blood BHB concentration within the therapeutic range of 2-5 mM. SIGNIFICANCE: Salivary BHB concentration strongly correlates with both serum and capillary blood BHB concentration. The POCT accurately measures salivary BHB concentration and provides a simple, user-friendly method to guide the use of KDT for children with drug-resistant epilepsy.

Indexed as

3-Hydroxybutyric AcidDiet, KetogenicDrug Resistant EpilepsySalivaAdolescentChildChild, PreschoolCohort StudiesFemaleHumansInfantMalePoint-of-Care TestingProspective Studies3-Hydroxybutyric Acidbeta‐hydroxybutyratedrug‐resistant epilepsyketogenic dietketonepoint‐of‐care testsaliva

Identifiers

PMID40411493
PMCPMC12455377

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.